Sildenafil

Product NDC

0179-0160

11-digit product format

001790160

Labeler code

0179

Product ID

0179-0160_7bea9cba-744c-4a27-e053-2a91aa0a4ecc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

sildenafil citrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

NDA021845

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-09-19

Marketing end

2020-07-31

Substance

SILDENAFIL CITRATE

Active strength

20 mg/1

Pharmacologic classes

Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record